Variant #0000682051 (NC_000023.10:g.119005968G>C, NM_004541.3:c.94G>C (NDUFA1))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.119005968G>C
DNA change (hg38) -
Published as NDUFA1(NM_004541.3):c.94G>C (p.(Gly32Arg)), NDUFA1(NM_004541.4):c.94G>C (p.G32R)
ISCN -
DB-ID NDUFA1_000003 See all 9 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00568 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFA1 NM_004541.3 -/. - c.94G>C r.(?) p.(Gly32Arg)
RNF113A NM_006978.2 -/. - c.-392C>G r.(?) p.(=)


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